| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264042 |
| Start |
241373136:241373136(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.29T>A |
| AA Mutation |
p.Val10Asp(p.V10D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264042 |
| Start |
241434288:241434288(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.998T>A |
| AA Mutation |
p.Val333Asp(p.V333D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000264042 |
| Start |
241475959:241475959(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2234G>A |
| AA Mutation |
p.Gly745Asp(p.G745D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |